| Literature DB >> 27622757 |
Ingrid Brezaniova1, Martin Hruby2, Jarmila Kralova3, Vladimir Kral1, Zulfiya Cernochova4, Peter Cernoch4, Miroslav Slouf4, Jana Kredatusova4, Petr Stepanek4.
Abstract
We developed fully biodegradable/metabolizable nanosystem based on polymer surfactant-stabilized thermoresponsive solid lipid nanoparticles with non-covalently bound photosensitizer temoporfin (T-SLNP) with particle size below 50nm. The efficacy of T-SLNP was compared with commercial temoporfin formulation in terms of in vitro phototoxicity in 4T1 (murine mammary carcinoma) and MDA-MB-231(human breast adenocarcinoma) cells and of in vivo anticancer effect in Nu/Nu mice bearing MDA-MB-231 tumors. In vitro study demonstrated faster accumulation kinetics in the cells for our formulation design resulting in higher phototoxicity against the tumor cells. In vivo anticancer efficacy was markedly improved by T-SLNP compared with commercial temoporfin formulation. Owing to controlled and sustained release properties, subcellular size, biocompatibility with tissue and cells, the T-SLNP nanodispersion prepared in this study represents promising drug delivery system applicable in cancer treatment.Entities:
Keywords: Drug delivery; Nanomedicine; Photodynamic therapy; Solid lipid nanoparticles; Temoporfin
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Year: 2016 PMID: 27622757 DOI: 10.1016/j.jconrel.2016.09.009
Source DB: PubMed Journal: J Control Release ISSN: 0168-3659 Impact factor: 9.776